UMAP-assisted $K$-means clustering of large-scale SARS-CoV-2 mutation datasets
Abstract
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has a worldwide devastating effect. The understanding of evolution and transmission of SARS-CoV-2 is of paramount importance for the COVID-19 control, combating, and prevention. Due to the rapid growth of both the number of SARS-CoV-2 genome sequences and the number of unique mutations, the phylogenetic analysis of SARS-CoV-2 genome isolates faces an emergent large-data challenge. We introduce a dimension-reduced -means clustering strategy to tackle this challenge. We examine the performance and effectiveness of three dimension-reduction algorithms: principal component analysis (PCA), t-distributed stochastic neighbor embedding (t-SNE), and uniform manifold approximation and projection (UMAP). By using four benchmark datasets, we found that UMAP is the best-suited technique due to its stable, reliable, and efficient performance, its ability to improve clustering accuracy, especially for large Jaccard distanced-based datasets, and its superior clustering visualization. The UMAP-assisted -means clustering enables us to shed light on increasingly large datasets from SARS-CoV-2 genome isolates.
Keywords
Cite
@article{arxiv.2012.15268,
title = {UMAP-assisted $K$-means clustering of large-scale SARS-CoV-2 mutation datasets},
author = {Yuta Hozumi and Rui Wang and Changchuan Yin and Guo-Wei Wei},
journal= {arXiv preprint arXiv:2012.15268},
year = {2021}
}
Comments
30 pages, 10 figures